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1 September 2000 Production of Diploid Eggs through Premeiotic Endomitosis in the Hybrid Medaka between Oryzias latipes and O. curvinotus
Yohei Shimizu, Naoki Shibata, Mitsuru Sakaizumi, Masakane Yamashita
Author Affiliations +

A hybrid medaka between Oryzias latipes and O. curvinotus spawns diploid eggs. We examined the cytological mechanisms of diploid egg formation in this hybrid. Oocytes in the hybrid passed through the first and second meiotic divisions and excluded two polar bodies, associated with reduction of the DNA content in oocytes. Each germinal vesicle in vitellogenic oocytes of the hybrid had 48 chromosomes with bivalent chiasmata, precisely twice the number of chromosomes in normal oocytes. These results suggest that before meiosis the chromosomes are doubled by mitosis without cytokinesis, that is, endomitosis, and that the resulting tetraploid oogonia undergo normal meiosis to produce diploid eggs. Except for a few vitellogenic oocytes that are probably derived from endomitotic oogonia, most oocytes were arrested at the zygotene stage in the hybrid ovary, suggesting the existence of checkpoint control that ensures the pairing of homologous chromosomes at prophase I, a situation differing from that in the male in which the checkpoint is at metaphase I. A sac-like structure was characteristic of the hybrid ovary. Although this structure was observed only in the hybrid, it may be a native component of the medaka ovary but difficult to observe because of its deformed outer structure due to enlargement of the inside oocytes. The present study confirms that this hybrid medaka provides a useful experimental system for investigations into the mechanisms of oogenesis and basic architecture of the ovary, which are difficult to analyze by using normal medaka.


Gametogenesis is a complex process that includes proliferation of germ cells, progression of meiotic cell division, and transformation into gametes (the egg and spermatozoon). Although spermatogenesis and oogenesis are cytologically identical in terms of meiosis, they differ in various aspects. For example, oocytes are arrested once at the diplotene stage of meiotic prophase I, during which substances (ex., mRNAs and yolk proteins) necessary for early embryonic development are accumulated (this stage being called vitellogenesis), whereas spermatocytes do not undergo such an arrest during meiosis. Critical checkpoint control must operate on the arrest of growing oocytes at the diplotene stage, but the entire mechanism still remains unclear in vertebrates.

Hybrids between closely related species often develop normally but become sterile or sometimes produce abnormal gametes. Like genetic mutants that are extensively used for analyzing other complex biological processes, appropriate hybrids are expected to provide a powerful tool for investigating the control mechanisms of gametogenesis, which are difficult to investigate by using normal organisms. In fact, 5 hybrid sterility loci have been identified using F1 hybrids between mouse species (Forejt, 1996). Among lower vertebrates, the medaka (genus Oryzias) is a useful model animal (Naruse et al., 1994), and the possibility of producing F1 hybrids from closely related species among the genus Oryzias has already been examined extensively (Iwamatsu et al., 1984, 1986, 1994; Sakaizumi, 1985, 1986; Uwa, 1986; Uwa and Parenti, 1988; Sakaizumi et al., 1992, 1993; Kurita et al., 1995). It is highly likely that we can gain an insight into the regulatory mechanisms of gametogenesis by investigating the cause of hybrid-specific abnormalities in the medaka.

The F1 hybrid between O. latipes and O. curvinotus exhibits sex-specific abnormalities; the male is sterile and the female lays diploid eggs (Hamaguchi and Sakaizumi, 1992; Sakaizumi et al., 1992, 1993). We have previously examined the process of spermatogenesis in this hybrid and found that meiosis stops just before metaphase I, probably due to incomplete chromosomal pairing (Shimizu et al., 1997). Nevertheless, spermiogenesis proceeds and sperm-like cells each having tetraploid (4C) DNA are produced without prior meiosis (Shimizu et al., 1997). The mature sperm-like cell has a large head and does not swim, causing male sterility (Hamaguchi and Sakaizumi, 1992).

Following the analyses of spermatogenesis in the hybrid medaka between O. latipes and O. curvinotus, we examined the cytological mechanisms of diploid egg formation in this hybrid. Histological observations and DNA fluorometry indicated that diploid eggs are produced through normal meiosis that follows an extra DNA replication by endomitosis occurring once in oogonia just prior to the premeiotic DNA replication.


Hybrid fish

Oryzias latipes from Suwa City, Nagano Prefecture, Japan and O. curvinotus from Hong Kong raised at Shinshu University were crossbred to generate inter-specific hybrids as described previously (Shimizu et al., 1997). The hybrid and parent medakas were cultured under reproductive conditions (14-hr light and 10-hr dark at 28°C).

Histological observation and DNA quantitation

Ovaries isolated from mature females were fixed in Bouin's solution, embedded in paraffin, serially sectioned at 5 μm, and stained with Carrazzi's hematoxylin and eosin to examine oogenesis histologically. Changes in morphology of spindles and chromosomes during meiosis were examined as follows (Iwamatsu, 1997). Ovaries were surgically removed from the fish 3 hr before light onset. Maturing oocytes that had undergone germinal vesicle breakdown were isolated from the ovary and cultured in medaka Ringer's solution (Iwamatsu, 1973) at room temperature. According to the schedule of meiosis (Iwamatsu, 1965; Yamauchi and Yamamoto, 1973), oocytes were fixed in medaka Ringer's solution containing 4% glutaraldehyde for 4 hr at 4°C for examining meiotic metaphase I, anaphase I, metaphase II and anaphase II. After fixation, the cortical cytoplasm at the animal pole was skinned from the underlying yolk mass using a scalpel in Ringer's solution and embedded in 1% agar. The agar blocks were embedded in paraffin, serially sectioned at 5 μm, and stained with Carrazzi's hematoxylin and eosin. Diameters of spindles at metaphases I and II were measured under a light microscope. For measuring DNA contents in oocytes, pieces of the cortical cytoplasm at the animal pole were placed on glass slides, stained with 1 μg/ml Hoechst 33258 dye in distilled water for 30 min at room temperature, and observed using a fluorescent microscope. Fluorescence intensity from Hoechst 33258 was measured using a P1 fluorometer (Nikon, Tokyo).

For observing chromosomes in vitellogenic oocytes, germinal vesicles (18 from 3 individuals of O. latipes and 54 from 15 individuals of the hybrid medaka) were isolated from the oocytes with forceps in Ringer's solution. After being washed by gentle pipetting, they were transferred into 1 μg/ml Hoechst 33258 dye on glass slides and examined under a fluorescence microscope.


Ovarian structure and oogenesis in the hybrid medaka

The ovarian cavity at the dorsal side of the hybrid ovary was well developed, as it is in the parent species (Fig. 1). The ovaries of the parent species contained many large, growing oocytes at the diplotene stage (Fig. 1A). In contrast, the ovary of the reciprocal hybrid had only a few growing oocytes at diplotene stage (Figs. 1B and C). In the hybrid ovary, we also found many sac-like components each consisting of a single layer of flattened somatic cells (Figs. 2 and 3B), which were not seen in the normal ovary (Fig. 3A). In the parent species, oogenesis progressed synchronously until the pachytene stage, where the oocytes clustered together, and supporting cells around the oocytes become follicle cells at the diplotene stage (Fig. 3A). In the hybrid, oogonia and zygotene oocytes were dominant in the sac-like structure (Fig. 3B). Somatic cells were also observed in the sac-like structure (Fig. 3B). A small number of diplotene oocytes found in the hybrid ovary existed mostly as single cells of various sizes (Figs. 1B and C), in striking contrast to those found in the parent species, which constituted groups in the ovary (data not shown).

Fig. 1

Hematoxylin-eosin (HE)-stained histological sections of ovaries from Oryzias latipes (A) and reciprocal hybrids, female O. latipes x male O. curvinotus (O. latipes-curvinotus, B) and female O. curvinotus x male O. latipes (O. curvinotus-latipes, C). Asterisks show the ovarian cavity, arrowheads show ovarian stroma, and arrows show growing oocytes at the diplotene stage in the hybrid medaka ovary. The ovarian cavity of O. curvinotus-latipes was damaged upon removal. Bar = 500 μm.


Fig. 2

An HE-stained section showing the sac-like structure in the hybrid medaka. The margins of the sac-like structure are indicated by arrowheads. The sac-like structure consists of a single layer of somatic cells. Growing oocytes at the diplotene stage (Od) are surrounded by follicle cells emerging from the sac-like structure. Bar = 50 μm.


Fig. 3

HE-stained sections showing germ cells in the normal (A) and the hybrid (B) medaka. In the ovary of the normal medaka (A), diplotene oocytes (Od) surrounded by follicle cells, pachytene oocytes (Op) clustered together, and premeiotic oogonia (Og) can be seen. In the hybrid medaka (B), most of oocytes fail to enter the pachytene stage, thereby remaining at the zygotene stage (Oz) in the sac-like structure. Numerous oogonia (Og) and some somatic cells (arrowheads) are also present in the sac-like structures. Bar = 25 μm.


Changes in chromosomes during meiosis in the hybrid medaka

In O. latipes oocytes, chromosomes were aligned at the first metaphase plate 2 hr before ovulation (Fig. 4A), and the first polar body was excluded 1 hr before ovulation (Fig. 4C). At the time of ovulation, chromosomes were aligned at the second metaphase plate (Fig. 4E), and by 15 min after insemination the second polar body was excluded (Fig. 4G). The observed time course of chromosome alignment and polar body exclusion was consistent with that described previously (Iwamatsu, 1965; Yamauchi and Yamamoto, 1973).

Fig. 4

HE-stained sections (A, C, E, G) and Hoechst 33258-stained specimens (B, D, F, H) showing spindles, polar bodies and chromosomes during meiosis in O. latipes. Metaphase I, A and B; anaphase I, C and D; metaphase II, E and F; anaphase II, G and H. Arrows show metaphase plates and arrowheads show polar bodies. Bar = 25 μm.


In the hybrid oocytes, the alignment of chromosomes at the first and second metaphase plates and the exclusion of the first and second polar bodies occurred on the same schedule as that in the normal eggs (Figs. 5A, C, E and G). However, the diameters of spindles formed at metaphases I and II in the hybrid oocytes were larger than those in the normal O. latipes oocytes (Table 1, p <0.01, Student's t-test). The difference between the spindle diameter of the normal and hybrid oocytes is due to the difference in the number of chromosomes present in the oocytes, as demonstrated later.

Fig. 5

HE-stained sections (A, C, E, G) and Hoechst 33258-stained specimens (B, D, F, H) showing spindles, polar bodies and chromosomes during meiosis in O. latipes-curvinotus. Metaphase I, A and B; anaphase I, C and D; metaphase II, E and F; anaphase II, G and H. Arrows show metaphase plates and arrowheads show polar bodies. Bar = 25 μm.


Table 1

The diameter of spindles in the oocytes at meiotic metaphase I and II (μm)


To obtain further information on the behavior of chromosomes during meiosis, we observed maturing oocytes after staining with the DNA dye Hoechst 33258. In O. latipes oocytes, chromosomes were aligned at metaphase I and II plates (Figs. 4B and F) and equally separated into two groups at anaphase I and II (Figs. 4D and H); one remained in the oocyte cytoplasm and the other was included in the polar bodies and eliminated from the oocytes. Chromosomal behavior during meiosis in the hybrid oocytes (Figs. 5B, D, F and H) was similar to that in O. latipes oocytes (Figs. 4B, D, F and H), but the number of chromosomes in the hybrid oocytes was apparently larger than that in the normal oocytes (compare Fig. 4 and 5).

Changes in DNA content during meiosis in the hybrid medaka

Cytological observations of maturing oocytes of the hybrid medaka strongly suggest that meiosis takes place normally in the hybrid oocytes. However, it has been reported that unreduced egg formation in a triploid crucian carp is due to abnormal meiosis resulting in the absence of reduction in DNA content during meiosis (Yamashita et al., 1993). To confirm actual reduction in DNA content during meiosis of the hybrid oocytes, we therefore investigated changes in DNA content by measuring the intensity of Hoechst 33258 fluorescence.

The hybrid oocytes at anaphase II contained twice the amount of DNA as compared with that in O. latipes (Table 2, p <0.01), consistent with the previous notion that the hybrid produces diploid eggs (Hamaguchi and Sakaizumi, 1992; Sakaizumi et al., 1992, 1993). DNA contents in the metaphase I and II oocytes in the hybrid were also significantly larger than those in O. latipes oocytes at the same phases (Table 2, p <0.05 for metaphase I and p <0.01 for metaphase II). Furthermore, DNA content was clearly reduced during meiosis in the hybrid, as well as in O. latipes, although the measured values did not completely fit to the expected values, which are 4, 2 and 1 at metaphase I, metaphase II and anaphase II, respectively, for the normal oocytes and 8, 4 and 2 for the hybrid oocytes (Table 2).

Table 2

Changes in DNA contents in the oocytes during meiosis (C)


Chromosome number in the hybrid oocytes

The DNA fluorometric study and the cytological observations indicated that there are already more chromosomes in hybrid oocytes at the beginning of meiosis and that meiosis itself proceeds normally with the reduction in DNA content by half after each of first and second meiotic divisions. To examine whether early-stage oocytes of the hybrid have an extra number of chromosomes, we counted the number of chromosomes in germinal vesicles of early diplotene oocytes. Each germinal vesicle of O. latipes contained 24 bivalent chromosomes having chiasmata, indicating that they are paired homologues (Fig. 6). The chromosomes in the hybrid oocytes were also bivalent with chiasmata, but their number was 48 (Fig. 7), precisely twice the number of chromosomes in the normal oocytes (Fig. 6).

Fig. 6

A Hoechst 33258-stained germinal vesicle of O. latipes oocyte at the diplotene stage. Different focal planes (A–C) of the same specimen showing 24 bivalents (arrowheads). Bar = 25 μm.


Fig. 7

A Hoechst 33258-stained germinal vesicle of O. latipescurvinotus oocyte at the diplotene stage. Different focal planes (A– C) of the same specimen showing 48 bivalents (arrowheads). Bar = 25 μm



Diploid eggs are produced by premeiotic endomitosis

Since the two sets of chromosomes in hybrids come from different species, pairing of homologous chromosomes is difficult. Indeed, our previous studies on spermatogenesis of the hybrid medaka between O. latipes and O. curvinotus indicated that most chromosomes do not pair at metaphase I (Shimizu et al., 1997). However, the present cytological observations together with DNA fluorometry have demonstrated that the hybrid oocytes are equipped with twice the number of chromosomes (48 vs. 24 in the normal oocytes) at the beginning of meiosis and that both first and second meiotic divisions proceed normally. We have also shown that all chromosomes in the germinal vesicles of the hybrid oocytes are bivalent with chiasmata, indicating that “homologous” chromosomes are present even in the hybrid. Taken together, the process of diploid egg production in the hybrid medaka is explainable as follows: First, oogonial chromosomes are doubled by endomitosis, the mitosis without cytokinesis, before entering meiosis, resulting in oogonia with pairs of identical chromosomes. Second, the tetraploid (4C) oogonia undergo premeiotic DNA replication and enter meiosis, producing oocytes with 8C DNA content, and, finally, normal meiotic division produces diploid (2C) eggs. A similar mechanism of unreduced egg formation has been found in Xenopus laevis and X. gilli hybrids (Kobel and DuPasquier, 1975) and in triploid fish (Cimino, 1972; Zhang et al., 1998) except for the triploid crucian carp Carassius auratus langsdorfii in which triploid eggs are produced by a defect in meiosis itself (Yamashita et al., 1993).

Type-B oogonia are connected by intercellular bridges (S. Hamaguchi, Niigata University, personal communication) and enter meiosis synchronously. Meiosis also proceeds synchronously. Thus, oocytes in normal medaka are observed as a cluster. In striking contrast to this, diplotene oocytes in the hybrid are found mostly as single cells of various sizes. These oocytes are probably derived from tetraploid oogonia produced by endomitosis. These findings suggest that after endomitosis the tetraploid oogonia do not divide mitotically any more. It is therefore likely that endomitosis occurs just before entry into meiosis.

Is endomitosis specific to hybrid females?

The female medaka constantly spawns a certain number of eggs every morning under appropriate conditions (Naruse et al., 1994). This indicates that the medaka ovary is equipped with a mechanism that organizes the entire process of oogenesis (proliferation of oogonia, entry into meiosis, vitellogenesis and maturation) by monitoring the number of germ cells at each process. The number of vitellogenic oocytes at the diplotene stage is considerably low in the hybrid ovary. If the above-proposed mechanism is in fact the mechanism that operates, it would force the hybrid ovary to produce oogonia and previtellogenic oocytes more actively in order to supply a sufficient amount of vitellogenic oocytes for coordinated oogenesis. Actually, the hybrid ovary contains unusually large numbers of previtellogenic oocytes, supporting the notion that early-stage germ cells are overproduced in the hybrid ovary. Endomitosis may occur only under such mis-regulated conditions. If so, endomitosis must be a phenomenon specific to the hybrid. In mammalian bone marrow, polyploid megakaryocytes (the precursors of platelets) are formed by endomitosis that is initiated by deficient activity of the M-phase-promoting kinase CDK1 due to the absence or very low levels of its regulatory subunit cyclin B1 (Vitrat et al., 1998). Whether similar mechanisms are responsible for endomitosis of the hybrid medaka oogonia remains to be investigated.

Another explanation for the occurrence of endomitosis in the hybrid is that endomitosis is not specific to the hybrid but occurs naturally in non-hybrid females at a very low frequency. Judging from the small number of the diplotene oocytes produced by endomitotic oogonia in the hybrid in which endomitosis is presumably enhanced by oogonial proliferation as discussed above, the frequency of endomitosis in the normal medaka, if it does occur, should be extremely low. In this case, it is unlikely that endomitosis itself causes any severe defects in viability or fecundity, thereby allowing the occurrence of endomitosis in the medaka from generation to generation. The spontaneous genomic duplication by inherent endomitosis may contribute to the evolution of medaka species to some extent. Further studies are required to verify whether endomitosis is the intrinsic characteristic of the normal medaka and, if so, we must clarify its biological significance.

Meiotic checkpoint differs in females and males

Most oocytes in the hybrid medaka cannot enter the pachytene stage of prophase I (present study, Hamaguchi and Sakaizumi, 1992). These oocytes fail to form paired chromosomes, as seen in spermatocytes (Shimizu et al., 1997). Synaptonemal complexes in these oocytes are also abnormal (Hamaguchi and Sakaizumi, 1992). On the other hand, endomitotically produced oocytes having paired chromosomes can enter the pachytene stage, as demonstrated in this study. Consequently, there must be a checkpoint monitoring the completion of chromosomal pairing at the zygotene stage. Several molecules that monitor recombination and synaptonemal complex formation have been discovered in some species. In the budding yeast Saccharomyces cerevisiae, mutations in molecules such as zip1, zip2, dmc1, sae3, and hop2 induce pachytene arrest (Bishop et al., 1992; Sym et al., 1993; McKee and Kleckner, 1997; Chua and Roeder, 1998; Tung and Roeder, 1998) and PCH2 is required for the meiotic checkpoint that prevents chromosome segregation when recombination and chromosome synapsis are defective (San-Segundo and Roeder, 1999). In addition, disruption of MLH1 or DMC1 in the mouse, which causes defective synapsis and/or recombination, results in the meiotic prophase I arrest (Edelmann et al., 1996; Pittman, et al., 1998; Yoshida et al., 1998). Since checkpoint mechanisms for proper meiotic chromosome segregation at prophase I seem to be widely conserved, it is most likely that similar checkpoints are also active in medaka oocytes.

In contrast to oogenesis, we previously showed that checkpoints are not active at prophase I, but are active at metaphase I, in spermatogenesis (Shimizu et al., 1997). Meiotic metaphase arrest was probably caused through monitoring chromosome alignment at the spindle equator as in mitosis (Rieder and Alexander, 1989). Thus, it is likely that some meiosis-specific checkpoints are active in oogenesis but silent in spermatogenesis, and vice versa. In this context, it is notable that sex chromosome recombination is suppressed during medaka spermatogenesis regardless of the chromosomal condition; even in sex-reversed XX males, sex chromosome recombination is suppressed as it is in the XY male (Matsuda et al., 1999). Probably, gamete-type-specific activation of checkpoints and regulation of meiotic recombination are related to this phenomenon.

Ovarian architecture revealed by the hybrid ovary

The ovarian folliclular structures and their endocrine functions have been investigated in the medaka (Sakai et al., 1988; Nagahama, 1994; Iwamatsu and Nakashima, 1996). However, information about the somatic architecture of the medaka ovary is extremely limited (Yamamoto, 1955; Kanamori et al., 1985). The present study showed that a sac-like structure is one of the most prominent features of the hybrid ovary. Then, what component(s) of the ovary does the sac-like structure originate from? During normal development of the medaka ovary, type-B oogonia and early oocytes at the leptotene to pachytene stages are surrounded by somatic cells forming a cystic structure. Accordingly, the cyst contains synchronously developing germ cells but no somatic cells. The sac-like structure contains several somatic cells and locally grouped oocytes of various stages, suggesting that it includes several cysts. Therefore, the possibility that the sac-like structure represents expansion of the cyst by a large number of early-stage oocytes is excluded. Considering that all somatic elements develop and function normally in the hybrid, somatic cells forming the sac-like structure might not be an abnormal response. Rather, this structure must exist in the normal ovary with the same topology as that in the hybrid, but its outer shape would be deformed by numerous growing oocytes and cannot be observed.

In conclusion, we found that diploid eggs laid by the hybrid female medaka are formed through normal meiosis from endomitotically produced tetraploid oogonia. We also revealed a difference in the checkpoints of meiosis between the male and female hybrids and the basic ovarian architecture that is difficult to define in the normal ovary. Given that the hybrid male is also a useful tool (Shimizu et al., 1997), our hybrid medaka furnishes a powerful experimental system for investigating the regulatory mechanisms of gametogenesis and the fundamental structure of gonads.


We are grateful to Dr. Satoshi Hamaguchi (Niigata University) for sharing unpublished data and encouragement throughout this study. We also thank Dr. Takashi Iwamatsu (Aichi University of Education) for providing valuable technical advice on the observation of medaka egg chromosomes. This work was supported by Grants-inAid for Scientific Research from the Ministry of Education, Science, Sports and Culture of Japan (No. 11236201 to MY and No. 11236206 to MS).



D. Bishop, D. Park, L. Xu, and N. Kleckner . 1992. DMC1: a meiosis-specific yeast homolog of E. coli recA required for recombination, synaptonemal complex formation, and cell cycle progression. Cell 69:439–456. Google Scholar


P. R. Chua and G. Roeder . 1998. Zip2, a meiosis-specific protein required for the initiation of chromosome synapsis. Cell 93:349–359. Google Scholar


M. C. Cimino 1972. The nuclear DNA content of diploid and triploid Poeciliopsis and other poecilid fishes with reference to the evolution of unisexual forms. Chromosoma 47:297–307. Google Scholar


W. Edelmann, P. E. Cohen, M. Kane, K. Lau, B. Morrow, S. Bennet, A. Umar, T. Kunkel, G. Gattoretti, R. Chagante, J. W. Pollard, R. D. Kolodner, and R. Kucherlapati . 1996. Meiotic pachytene arrest in MLH1-deficient mice. Cell 85:1125–1134. Google Scholar


J. Forejt 1996. Hybrid sterility in the mouse. Trend Genet 12:412–417. Google Scholar


S. Hamaguchi and M. Sakaizumi . 1992. Sexually differentiated mechanisms of sterility in interspecific hybrids between Oryzias latipes and O. curvinotus. J Exp Zool 263:323–329. Google Scholar


T. Iwamatsu 1965. A further study on fertilizability of fish oocytes. Annot Zool Japan 38:190–197. Google Scholar


T. Iwamatsu 1973. Studies on oocyte maturation in the medaka, Oryzias latipes. Improvement of culture medium for oocyte in vitro. Jpn J Ichthyol 20:218–224. in Japanese. Google Scholar


T. Iwamatsu 1997. Abbreviation of the second meiotic division by precocious fertilization in fish oocyte. J Exp Zool 277:450–459. Google Scholar


T. Iwamatsu and S. Nakashima . 1996. Dynamic growth of oocytes of the medaka, Oryzias latipes. I. A relationship between establishment of the animal-vegetal axis of the oocyte and its surrounding granulosa cells. Zool Sci 13:873–882. Google Scholar


T. Iwamatsu, H. Uwa, A. Inden, and K. Hirata . 1984. Experiments on interspecific hybridization between Oryzias latipes and Oryzias celebensis. Zool Sci 1:653–663. Google Scholar


T. Iwamatsu, T. Watanabe, R. Hori, T. J. Lam, and O. P. Saxena . 1986. Experiments on interspecific hybridization between Oryzias melastigma and Oryzias javanicus. Zool Sci 3:287–293. Google Scholar


T. Iwamatsu, T. Mori, and R. Hori . 1994. Experimental hybridization among Oryzias species. I. O. celebensis, O. javanicus, O. latipes, O. luzonensis and O. melastigma. Bull Aichi Univ Educ 43:Nat. Sci. 103–112. Google Scholar


A. Kanamori, Y. Nagahama, and N. Egami . 1985. Development of the tissue architecture in the gonads of the medaka Oryzias latipes. Zool Sci 2:695–706. Google Scholar


H. R. Kobel and L. DuPasquier . 1975. Strains and species of Xenopus for immunological research. In “Developmental Immunology”. Ed by J. B. Solomon and J. D. Horton , editors. Elsevier/North-Holland Biomedical Press. Amsterdam. pp. 299–306. Google Scholar


J. Kurita, T. Oshiro, F. Takashima, and M. Sakaizumi . 1995. Cytogenetic studies on diploid and triploid oogenesis in interspecific hybrid fish between Oryzias latipes and O. curvinotus. J Exp Zool 273:234–241. Google Scholar


M. Matsuda, S. Sotoyama, S. Hamaguchi, and M. Sakaizumi . 1999. Male-specific restriction of recombination frequency in the sex chromosomes of the medaka, Oryzias latipes. Genet Res Camb 73:958 225–231. Google Scholar


A. H. McKee and N. Kleckner . 1997. Mutations in Saccharomyces cerevisiae that block meiotic prophase chromosome metabolism and confer cell cycle arrest at pachytene identify two new meiosis-specific genes SAE1 and SAE3. Genetics 146:817–834. Google Scholar


Y. Nagahama 1994. Endocrine regulation of gametogenesis in fish. Int J Dev Biol 38:217–229. Google Scholar


K. Naruse, M. Sakaizumi, and A. Shima . 1994. Medaka as a model organism for research in experimental biology. Fish Biol J MEDAKA 6:47–52. Google Scholar


D. L. Pittman, J. Cobb, K. J. Schiment, L. A. Wilson, D. M. Cooper, E. Brignull, M. A. Handel, and J. S. Schimenti . 1998. Meiotic prophase arrest with failure of chromosome synapsis in mice deficient for Dmc1, a germline-specific RecA homolog. Mol Cell 1:697–705. Google Scholar


C. L. Rieder and M. A. Alexander . 1989. The attachment of chromosomes to the mitotic spindle and the production of aneuploidy in newt lung cells. In “Mechanisms of Chromosome Distribution and Aneuploidy”. Ed by M. A. Resnick and B. K. Vig , editors. Alan R Liss Inc. New York. pp. 185–194. Google Scholar


N. Sakai, T. Iwamatsu, K. Yamauchi, N. Suzuki, and Y. Nagahama . 1988. Influence of follicular development on steroid production of the medaka (Oryzias latipes) ovarian follicle in response to exogenous substances. Gen Comp Endocrinol 71:516–523. Google Scholar


M. Sakaizumi 1985. Electrophoretic comparison of proteins in five species of Oryzias (Pisces: Oryziatidae). Copeia 1985:521–522. Google Scholar


M. Sakaizumi 1986. Genetic divergence in wild populations of medaka, Oryzias latipes (Pisces: Oryziatidae) from Japan and China. Genetica 69:119–125. Google Scholar


M. Sakaizumi, Y. Shimizu, and S. Hamaguchi . 1992. Electrophoretic studies of meiotic segregation in inter- and intraspecific hybrids among east Asian species of the genus Oryzias (Pisces: Oryziatidae). J Exp Zool 264:85–92. Google Scholar


M. Sakaizumi, Y. Shimizu, T. Matsuzaki, and S. Hamaguchi . 1993. Unreduced diploid eggs produced by interspecific hybrids between Oryzias latipes and O. curvinotus. J Exp Zool 266:312–318. Google Scholar


P. A. San-Segundo and G. S. Roeder . 1999. Pch2 links chromatin silencing to meiotic checkpoint control. Cell 97:313–324. Google Scholar


Y. H. Shimizu, N. Shibata, and M. Yamashita . 1997. Spermiogenesis without preceding meiosis in the hybrid medaka between Oryzias latipes and O. curvinotus. J Exp Zool 279:102–112. Google Scholar


M. Sym, J. Engebrecht, and G. S. Roeder . 1993. ZIP1 is a synaptonemal complex protein required for meiotic chromosome synapsis. Cell 72:365–378. Google Scholar


K. S. Tung and G. S. Roeder . 1998. Meiotic chromosome morphology and behavior is zip1 mutants of Saccharomyces cerevisiae. Genetics 149:817–832. Google Scholar


H. Uwa 1986. Karyotype evolution and geographical distribution in the ricefish, genus Oryzias (Oryziidae). In “Indo-Pacific Fish Biology: Proceedings of the Second International Conference on Indo-Pacific Fishes”Ed by T. Uyeno, R. Arai, T. Taniuchi, and K. Matsuura , editors. Ichthyological Society of Japan. Tokyo. pp. 867–876. Google Scholar


H. Uwa and L. R. Parenti . 1988. Morphometric and meristic variation in ricefishes, genus Oryzias: a comparison with cytogenetic data. Japan J Ichthyol 35:159–166. Google Scholar


N. Vitrat, K. Cohen-Solal, C. Pique, J. P. Le Couedic, F. Norol, A. K. Larsen, A. Katz, W. Vainchenker, and N. Debili . 1998. Endomitosis of human megakaryocytes are due to abortive mitosis. Blood 91:3711–3723. Google Scholar


T. Yamamoto 1955. Morphological and cytological studies on the oogenesis of the fresh-water fish, medaka (Oryzias latipes). Gyoruigakuzasshi 4:170–181. in Japanese. Google Scholar


M. Yamashita, J. Jiang, H. Onozato, T. Nakanishi, and Y. Nagahama . 1993. A tripolar spindle formed at meiosis I assures the retention of the original ploidy in the gynogenetic triploid crucian carp, Carassius auratus langsdorfii. Dev Growth Differ 35:631–636. Google Scholar


K. Yamauchi and K. Yamamoto . 1973. In vitro maturation of the oocytes in the medaka, Oryzias latipes. Annot Zool Japon 46:144–153. Google Scholar


K. Yoshida, G. Kondoh, Y. Matsuda, T. Habu, Y. Nishimune, and T. Morita . 1998. The mouse RecA-like gene Dmc1 is required for homologous chromosome synapsis during meiosis. Mol Cell 1:707–718. Google Scholar


Q. Zhang, K. Arai, and M. Yamashita . 1998. Cytogenetic mechanisms for triploid and haploid egg formation in the triploid loach Misgurnus anguillicaudatus. J Exp Zool 281:608–619. Google Scholar
Yohei Shimizu, Naoki Shibata, Mitsuru Sakaizumi, and Masakane Yamashita "Production of Diploid Eggs through Premeiotic Endomitosis in the Hybrid Medaka between Oryzias latipes and O. curvinotus," Zoological Science 17(7), 951-958, (1 September 2000).
Received: 3 April 2000; Accepted: 1 May 2000; Published: 1 September 2000
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